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Conversion of unsaturated fatty acids-nucleophilic additions to methyl (E)-12-oxo-10-octadecenoate [1]

Author
MALETZ, R; SCHÄFER, H. J; QUERMANN, R1
[1] Organisch-Chemisches Institut der Universität Münster, Germany
Source

Fett (Weinheim). = Lipid. 1996, Vol 98, Num 11, pp 370-379 ; ref : 37 ref

CODEN
FWTEEG
ISSN
0931-5985
Scientific domain
Food science technology; Chemical industry parachemical industry
Publisher
Wiley-VCH, Weinheim
Publication country
Germany
Document type
Article
Language
English
Keyword (fr)
Acide gras insaturé Addition nucléophile Composé aliphatique Composé éthylénique Cétoacide Hydroxyacide Oxydation Réactivité chimique Stéréoisomère trans Synthèse chimique Octadéc-10-énoïque acide(12-oxo) ester méthyle Ricinoléique acide ester méthyle
Keyword (en)
Unsaturated fatty acid Nucleophilic addition Aliphatic compound Ethylenic compound Ketoacid Hydroxyacid Oxidation Chemical reactivity Trans stereoisomer Chemical synthesis
Keyword (es)
Acido graso no saturado Adición nucleófila Compuesto alifático Compuesto etilénico Cetoácido Hidroxiácido Oxidación Reactividad química Estereoisómero trans Síntesis química
Classification
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C02 Aliphatic compounds

Discipline
Organic chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
2516970

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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